Mengbo Zhu1,2†
Wenbin Xu2†Jiuzhou Jiang2†
Yining Wang3†
Yanjing Guo1,4Ruijia Yang1,4Yaqiong Chang1Bin Zhao1Zhenyu Wang1Jianfeng Zhang2Te Wang3*Liqin Shangguan2*
Shaowei Wang1,4*- 1Department of Orthopedic, Second Hospital of Shanxi Medical University, Taiyuan, China
- 2Department of Orthopedic Surgery, Sir Run Run Shaw Hospital, Medical College of Zhejiang University, Hangzhou, China
- 3Department of Orthopaedics, The Second Affiliated Hospital and Yuying Children’s Hospital of Wenzhou Medical University, Wenzhou, China
- 4Department of Biochemistry, Basic Medical College, Shanxi Medical University, Taiyuan, China
Osteoclasts (OCs) play an important role in osteoporosis, a disease that is mainly characterized by bone loss. In our research, we aimed to identify novel approach for regulating osteoclastogenesis and thereby treating osteoporosis. Previous studies have set a precedent for screening traditional Chinese herbal extracts for effective inhibitors. Peiminine is an alkaloid extracted from the bulb of Fritillaria thunbergii Miq that reportedly has anticancer and anti-inflammatory effects. Thus, the potential inhibitory effect of peiminine on OC differentiation was investigated via a series of experiments. According to the results, peiminine downregulated the levels of specific genes and proteins in vitro and consequently suppressed OC differentiation and function. Based on these findings, we further investigated the underlying molecular mechanisms and identified the NF-κB and ERK1/2 signaling pathways as potential targets of peiminine. In vivo, peiminine alleviated bone loss in an ovariectomized mouse model.
Introduction
Osteoporosis, common in elderly individuals, especially women, is characterized mainly by microarchitectural degeneration of the trabeculae and intrinsic bone tissues as well as pathological bone remodeling (1). Due to these pathological changes, which are often described as bone loss, patients suffering from osteoporosis are at an enhanced risk for osteoporosis-related fractures (2). A critical cause of bone loss is the imbalance between bone formation and osteoclast (OC)-related bone resorption (3). Estrogen replacement therapy (ERT) is considered to be effective for menopausal osteoporosis but increases the risk of endometrial cancer, breast cancer, and asthma (4, 5), and bisphosphonates are the mainstays for the in-clinical treatment of osteoporosis. However, bisphosphonates exhibit nephrotoxicity, hepatic toxicity, and alimentary canal toxicity (6). Thus, we expect to explore safer strategies for regulating the differentiation of OCs to treat osteoporosis. Natural compounds with a broad spectrum of biological activity and limited side-effects have become the main targets of our research. There have been many studies on the treatment of osteoporosis using natural compounds (7–9) that have provided us with a reliable theoretical and technological basis for our exploration into the field.
Peiminine is an alkaloid extracted from the bulb of Fritillaria thunbergii Miq, a traditional Chinese medicinal herb (for the chemical structure of peiminine, see Figure 1A) (10). A study performed in 2018 reported that peiminine exerted a protective effect on lipopolysaccharide-induced mastitis by repressing signaling pathways such as protein kinase B (Akt), nuclear factor-κB (NF-κB), and mitogen-activated protein kinases (MAPKs) (11), and peiminine was shown to similarly protect dopaminergic neurons from neuroinflammation by inhibiting the extracellular-regulated protein kinase (ERK1/2) and NF-κB pathways in another study (12). The process of osteoclastogenesis shares these pathways.
Figure 1 Peiminine dose-dependently inhibits osteoclastogenesis induced by RANKL and is not cytotoxic in vitro. (A) The molecular structure of peiminine. (B) Evaluation of the cytotoxicity of peiminine by the CCK-8 assay. n= 5, (C) TRAP staining of OCs treated with peiminine at every concentration. (D) Quantitative analysis of the TRAP-positive cells with more than 3 nuclei in each well of a 96-well plate. n= 5, *P < 0.05, ***P < 0.001. (E) Fluorescence staining images of OCs treated without or with peiminine at different concentrations (5 µmol/L and 10 µmol/L). The scale bar is 200 µm. (F) Analysis of the average number of OC nuclei (dots with blue fluorescence indicated by DAPI staining). n= 5, ***P < 0.001.
OCs are multinuclear giant cells derived from bone marrow monocytes (BMMs) (13), and the receptor activator of nuclear factor-κB ligand (RANKL)-receptor activator of nuclear factor-κB (RANK)-osteoprotegerin (RANK-RANKL-OPG) signaling pathway is the most influential mechanism known to regulate the process of OC differentiation (3, 13–15). Groping towards this way, NF-κB and ERK pathways are all crucial downstream signaling pathways of RANKL-RANK axis (16–18). Hence, blocking these pathways is probably a promising direction of osteoporosis treatment.
We herein hypothesized that peiminine exerts similar inhibitory effects on osteoclastogenesis. Besides, many previous studies have reported that peiminine has certain anticancer effects (19, 20) and is also effective against acute and chronic inflammatory injury (21–24). In the context of orthopedic diseases, peiminine is known to protect articular cartilage from destructive cytokines (25), but its inhibitory effect on OCs and its effect on bone loss have not yet been reported. Thus, this study aimed to provide a novel and comprehensive solution for combating degenerative and aging-related bone diseases.
In our study, we found for the first time that peiminine suppressed osteoclastogenesis by inhibiting the NF-κB signaling pathway. The expression of OC-related genes and proteins was measured to evaluate the influence of peiminine on OC differentiation and function. Our results indicated the alleviating promise of peiminine for osteolytic bone diseases, and its effect on bone loss alleviation was confirmed by animal experiments in vivo. The results obtained from a mouse model of osteoporosis induced by estrogen deficiency indicated the potential of peiminine as an alleviating option for osteoporosis.
Methods and Materials
Cell Culture
The indispensable basic cell culture materials were produced by Thermo Fisher Scientific (Carlsbad, CA, USA), including alpha-modified minimal essential medium (α-MEM), penicillin/streptomycin (P/S), and fetal bovine serum (FBS). We extracted BMMs from the tibias and femur marrow of C57BL/6 mice at 6 weeks of age in accordance with the National Institutes of Health (NIH) Guide for the Care and Use of Laboratory Animals and the guidelines for The Laboratory Animal Center of Sir Run Run Shaw Affiliated Hospital of Zhejiang University School of Medicine (Hangzhou, Zhejiang).
Under sterile conditions, 6-week-old mice were sacrificed, and their tibias and femurs were immediately harvested. The two ends of the bones (osteoepiphysis) were clipped to expose the bone marrow, which was harvested from the diaphysis via a 1 ml syringe and placed into medium. After triturating with a pipette, M-CSF was added to the bone marrow cell suspension for BMM sorting. The suspended cells were discarded after 48 h of culture in the presence of M-CSF, and the adherent cells were deemed the BMMs. The medium was comprised of α-MEM, 1% (v/v) P/S, 10% (v/v) FBS, and 50 ng/ml M-CSF.
Evaluation of Peiminine Efficacy and Toxicity
BMMs were seeded in plates (96-well plate) at a concentration of 8×103 cells per well and cultured in α-MEM (Thermo Fisher Scientific, CA, USA) supplemented with 50 ng/ml M-CSF (R&D Systems, MN, USA) overnight according to the method published by Jin and Chen in 2019 (7, 26). After adherence, the BMMs were stimulated with GST-rRANKL (50 ng/ml) (R&D Systems, MN, USA), and peiminine (Feiyubio, Jiangsu, China, CAS no. 18059-10-4) was added to the cultured cells at varying concentrations (1, 2.5, 5, and 10 μmol/L). The medium was changed every 2 days, and GST-rRANKL and the drug were refreshed every 2 days until the sixth day, when OCs formed. The differentiated OCs were stained with tartrate-resistant acid phosphatase (TRAP) (Sigma-Aldrich Corp., St. Louis, MO, USA) solution after fixation with 2.5% glutaraldehyde (DAMAO chemical reagent factory, Tianjin, China) for 15 min, and the number of cells in each well was then counted under a bright-field optical microscope (Olympus, Tokyo, Japan). Cells with three or more nuclei were considered OCs, and the number of TRAP-positive multinucleated cells was used to indicate the differentiation of OCs.
Additionally, the response of the cells to increasing concentrations of peiminine (1, 2.5, 5, and 10 μmol/L) was assessed. BMMs were treated with varying concentrations of peiminine for 5 days, after which 20 μl of WST-8 solution (Cell Counting Kit-8; Dojindo Laboratories, Kumamoto, Japan) was added to the wells for another 4 h. The absorbance at 450 nm was measured by the enzyme-linked immunosorbent assay (Thermo Fisher Scientific, Waltham, MA, USA).
Fluorescence Staining
BMMs were seeded in 96-well plates (8×103 cells per well) and cultured in α-MEM containing M-CSF (50 ng/ml) for 24 h; after adherence, the medium was replaced in each well. The control group BMMs were cultured in α-MEM containing M-CSF (50 ng/ml) and GST-rRANKL (50 ng/ml) for 6 days, while the BMMs in the two experimental groups were cultured in α-MEM containing M-CSF (50 ng/ml), GST-rRANKL (50 ng/ml), and peiminine (5 and 10 μmol/L separately) for 6 days (medium refreshed every 2 days). On the seventh day after cell seeding, the cells were fixed with 4% paraformaldehyde, and the membrane permeability was increased with 0.5% Triton X-100 (Sigma-Aldrich Corp., St. Louis, MO, USA).
F-actin filaments were stained with rhodamine phalloidin (Thermo Fisher Scientific, Waltham, MA, USA) after blocking with 5% bovine serum albumin. According to the manufacturer’s instructions, the vial contents were dissolved in 150 µl of anhydrous DMSO to yield a 400× stock solution at a concentration of 2,000 assays/ml, which was equivalent to approximately 66 µM. During the experiment, 0.5 µl of the 400× stock solution was diluted in 200 µl of PBS, and approximately 100 µl was added to each well. After 45 min of staining, the cells were washed with PBS and stained with DAPI, and the results were observed with a fluorescence microscope (CKX53; Olympus, Tokyo, Japan). The numbers of multinucleated cells and nuclei in each multinucleated cell were counted under a fluorescence microscope, and the average number of nuclei in each well was then calculated.
Bone Resorption Assay In Vitro
First, sterile bone slices were placed on the well bottoms of 96-well plates, after which BMMs were seeded onto the bone slices (1×104 cells per well) and cultured in α-MEM containing M-CSF (50 ng/ml) for 24 h; after adherence, the medium in each well was replaced. The negative control group cells were cultured in α-MEM containing M-CSF (50 ng/ml), while those in the positive control group were cultured in α-MEM supplemented with M-CSF (50 ng/ml) and GST-rRANKL (50 ng/ml), and those in the two experimental groups were cultured in α-MEM supplemented with M-CSF (50 ng/ml), GST-rRANKL (50 ng/ml), and peiminine (5 and 10 μmol/L). The cells in all groups were cultured for 14 days, and the medium was changed every 2 days. On the 15th day after cell seeding, the cell cultures were removed, and the bone slices from the different groups were obtained.
To prepare scanning electron microscopy (SEM) samples, adherent cells were removed from the bone slices by washing with 75% alcohol and trypsin to ensure that the bone slices were completely decellularized. Then, these decellularized bone slices were fully dried and covered with conductive carbon powder with a vacuum spray plating device (JEOL Ltd., Japan) prior to SEM. The resorption pits on the dried bone slices were observed by SEM (TM-1000; Hitachi, Tokyo, Japan). ImageJ software was used to measure the gross resorption pit areas as follows: adjust the scanning picture to 8-bit and set an appropriate gray value threshold; select dark recessed areas as the resorption area and deselect all scratch-like recessed areas (scratches were engendered during the process of slice cutting); and calculate the gross resorption pit areas in each well.
Real-Time Quantitative Polymerase Chain Reaction
BMMs were seeded in 6-well plates (15×104 cells per well) and cultured in α-MEM containing M-CSF (50 ng/ml) for 24 h; after adherence, the medium in each well was changed. Cells in the negative control group were cultured in α-MEM containing M-CSF (50 ng/ml), while those in the positive control group were cultured in α-MEM containing M-CSF (50 ng/ml) and GST-rRANKL (50 ng/ml), and those in the two experimental groups were cultured in α-MEM containing M-CSF (50 ng/ml), GST-rRANKL (50 ng/ml), and peiminine (5 and 10 μmol/L). Cells in all the groups were cultured for 6 days, and the medium was changed every 2 days. On the seventh day after cell seeding, total RNA was extracted from the cells with TRIzol reagent and the Ultrapure RNA Kit (DNase I) (CW Biotech, Beijing, China).
The RNA concentration in each sample was detected by measuring the absorbance at 260 nm with a spectrophotometer (Thermo Fisher Scientific, Waltham, MA, USA). Evo M-MLV RT Premix for qPCR (Accurate Biotechnology, Hunan, China) was used to reverse transcribe the total RNA (500 ng) into single-stranded cDNA.
According to the manufacturer’s protocol, the expression of the target genes was determined with a SYBR polymerase chain reaction Master Mix Kit (Yeasen Co., Shanghai, China) on the ABI QuantStudio 6 Real-Time PCR System (Thermo Fisher Scientific, Waltham, MA, USA). The relative expression levels of the target genes were analyzed by the 2−ΔΔCq method, and the expression level of the mouse glyceraldehyde-3-phosphate dehydrogenase (GAPDH) gene was used as the normalization parameter in our analysis. The primer sequences are listed in Table 1.
Table 1 Primer sequences used in qRT-PCR.
Western Blot Analysis
To evaluate the expression of proteins related to the NFATc1 signaling pathway and bone resorption, BMMs were seeded in six-well plates (1.5×105 cells per well) overnight and allowed to adhere. The cells were cultured with or without peiminine (10 μmol/L) in medium containing M-CSF (50 ng/ml) and GST-rRANKL (50 ng/ml), and total proteins were then harvested separately from each well on days 0, 1, 3, and 5. Radioimmunoprecipitation assay (RIPA) lysis buffer (consisting of phosphatase inhibitors, 500 g/ml DNase I, and 100 g/ml PMSF) was used to extract the total protein.
To assess the expression of signaling pathway-related proteins at early time points, BMMs were seeded at a density of 5×105 cells per well in six-well plates and incubated in GST-rRANKL-free medium overnight. The cells were starved for more than 6 h and then pretreated with peiminine for 2 h. GST-rRANKL (50 ng/ml) was then added to each well, and total protein was harvested in RIPA buffer at the following time points: 0, 10, 20, 30, and 60 min.
The proteins were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (10%), transferred onto nitrocellulose membranes, and blocked with 5% BSA for 2 h. The membranes were incubated with the following primary antibodies: anti-c-Fos (1:1,000, Cat. #2250), anti-NF-κB (anti-p65) (1:1,000, Cat. #8242), anti-phospho-NF-κB (anti-pp65) (1:1,000, Cat. #3033), anti-NFATc1 (1:1,000, Cat. #sc-7294), anti-integrin β3 (1:1,000, Cat. #sc-365679), anti-cathepsin K (CTSK) (1:1,000, Cat. #sc-48353), anti-ATP6v0s2 (1:1,000, Cat. #sc-69108), anti-p-IκB-α (1:1,000, Cat. #sc-8404), and anti-β-actin (1:5,000, Cat. #sc-47778), anti-phospho-ERK1/2 (1:1,000, Cat. #AF1015), anti-ERK1/2 (1:1,000, Cat. #AF0155), anti-phospho-P38 (1:1,000, Cat. #AF4001), anti-P38 (1:1,000, Cat. #AF6456).
Primary antibodies specific for c-Fos, phospho-NF-κB (pp65), and NF-κB (p65) were acquired from Cell Signaling Technology (Beverly, MA, USA). Primary antibodies specific for NFATc1, integrin β3, CTSK, V-ATPase-d2 (ATP6v0d2), phosphorylated iκB (p-IκB)-α, and β-actin were obtained from Santa Cruz Biotechnology (San Jose, CA, USA). Primary antibodies specific for ERK1/2, phospho-ERK1/2, phospho-P38, and P38 were acquired from Affinity Biosciences (Jiangsu, China).
The membranes were incubated with primary antibodies at 4°C for more than 12 h and then with secondary antibodies conjugated to horseradish peroxidase at room temperature for more than 2 h. Immunoreactive bands were visualized with the Touch Imaging System made by Bio-Rad (ChemiDoc™, Bio-Rad, CA, USA).
The relative protein content was calculated with ImageJ software as follows: adjust the protein band images to 8-bit and obtain clean protein bands using the Subtract Background function; use the Measurement function to calculate the gray value of each band; divide the gray values of the control proteins by the gray values of the corresponding target proteins to determine the relative protein amounts.
Ovariectomy Mouse Model
Female 10-week-old C57BL/6 mice (n=30), acquired from the Animal Experimental Center of Sir Run Run Shaw Hospital (Zhejiang, China), were randomly separated into three groups: the sham group (control group) (n=10), the OVX group (n=10), and the intervention group (n=10). Mice from the OVX and intervention groups were ovariectomized according to the method published by Zhou in 2016 (27). As a control, mice in the sham group underwent a sham operation; mice in the intervention group were treated with peiminine (10 mg/kg), while those in the OVX and sham groups were injected with PBS.
All mice were housed in ventilated and sterilized cages and subjected to surgery after adaptive feeding for 1 week. Each of these specific pathogen-free cages held five mice. Seven days after the surgery, mice in the OVX and sham groups were administered PBS, while those in the intervention group were intraperitoneally injected with peiminine (10 mg/kg) every 2 days for 6 weeks. All the mice survived and were healthy in the interim. At the seventh week after surgery, all the mice were sacrificed, and their femurs were harvested for histological and micro-CT (μCT) analysis.
µCT Scanning of Mouse Femurs
We measured the following parameters of mouse femur samples: the bone volume/tissue volume ratio (BV/TV), trabecular number (Tb. N), trabecular separation (Tb. Sp), and trabecular thickness (Tb. Th). Samples were scanned with a BRUKER skyscan1176 μCT instrument (Bruker Daltonic Inc. USA) after fixation with 4% paraformaldehyde for 1 day (24 h). The μCT setup was as follows: 50 kV scanning voltage, 500 μA scanning current, 9 μm spatial resolution, and 1,600 × 2,672-pixel image matrix. Then, a 1-mm-high area 0.5 mm beneath the growth plate was designated for qualitative and quantitative analysis. N-Recon software was used for three-dimensional image rebuilding, and CT-AN software was used for quantitative analysis.
Histological Staining
Left femur samples from all mice were fixed in 4% paraformaldehyde for 2 days (48 h) and then decalcified by 14% EDTA at 37°C for 14 days (9). Sagittal paraffin sections at thickness of 5 μm were obtained from the decalcified bone tissues. Representative images of TRAP staining and hematoxylin and eosin (H&E) staining were collected, and the claret red cells around the resorbed bone were considered TRAP-positive OCs. In addition, we assessed the OCs surface (OC. S) and bone surface (BS) by measuring the TRAP-positive cells’ perimeters and bone perimeters separately.
Statistical Analysis
In the Results section, all quantitative data are presented as the mean ± standard deviation. Statistical analyses were conducted using one-way analysis of variance (ANOVA) followed by Tukey’s post hoc test with GraphPad Prism 8. All data are presented as the means ± SDs; *P < 0.05, **P < 0.01, ***P < 0.001 compared to the control.
Results
Peiminine Is Not Toxic in BMMs and Suppresses OC Formation and Fusion Induced by RANKL
Before assessing the inhibitory effect of peiminine on osteoclastogenesis, we investigated its cytotoxicity. The CCK-8 assays confirmed that the reduction in the number of OCs was not due to BMM cytotoxicity, as the number of live cells did not differ after treatment with varying concentrations of peiminine as determined by absorbance detection (Figure 1B). The number of cells in each group did not change significantly in the presence of various concentrations of peiminine, indicating that peiminine had no toxic effect on living BMMs (1 μmol/L group: p= 0.0665; 1 μmol/L: p= 0.0503; 5 μmol/L: p= 0.0909; 10 μmol/L: p=0.0682; 20 μmol/L: p=0.3824; 40 μmol/L: p=0.3174).
To evaluate the inhibitory effect of peiminine on the generation of OCs, TRAP staining was used to assess the cellular responses to increasing peiminine concentrations (1, 2.5, 5, and 10 μmol/L). As shown in Figures 1C, D, the number of TRAP-positive OCs in each well was dose-dependently decreased, and significantly fewer multinuclear TRAP-positive cells were observed in the cells treated with 10 μmol/L peiminine than in untreated cells (p= 2.04798E-09). Similarly, the numbers of cells treated with 1, 2.5, and 5 mol/L peiminine were obviously decreased (1 μmol/L: p= 0.0129; 2.5 μmol/L: p= 6.93569E-06; 5 μmol/L: p= 1.27028E-08).
Additionally, to determine whether peiminine disrupts the cellular fusion of OCs, fluorescence staining was performed to assess their fusion and the quantity of nuclei in every multinucleated cell. Figures 1E, F show that cell fusion was reduced in the presence of 5 and 10 μmol/L peiminine, which is consistent with the TRAP staining results. Specifically, the number of nuclei per OC was markedly decreased (5 μmol/L: p= 0.0004652; 10 μmol/L: p= 9.86236E-05).
The Inhibitory Effect of Peiminine Is Time-Dependent
In addition, BMMs were treated with peiminine on days 1–3, 3–5, 5–6, and 1–6 to assess its inhibitory effect at various stages of OC differentiation. In Figure 2A, the pink boxes represent the time points of the dosing. Compared with the control group, peiminine had a notable inhibitory effect in all treatment groups. The number of OCs in the 1–6day group was dramatically lower than that in the control group (p=0.00000060), and those in the remaining groups were lower than that in the control group (1–3day group: p= 0.00000175; 3–5day group: p= 0.0000189; 5–6day group: p= 0.00636).
Figure 2 Peiminine has a suppressive effect on OC formation at different time points. (A) BMMs were treated with peiminine on days 1–3, 3–5, 5–6, and 1–6. (B) Quantitative analysis of the OC numbers in groups with different administration times (TRAP-positive cells were counted as OCs). n= 5, *P < 0.05, **P < 0.01, ***P < 0.001. (C) Representative images of the TRAP-positive cells in the different administration time groups.
Moreover, direct comparisons of the treatment groups revealed that the effect of peiminine was limited on days 5–6, as the number of OCs in the 5–6day group was higher than that in the other treatment groups (1–3day group: p= 0.019; 3–5day group: p= 0.049; 1–6day group: p= 0.001). Additionally, peiminine exerted an optimal inhibitory effect on the 1–6day group, as the OC number was lower than that in the other groups (1–3 group: p= 0.002; 3–5 group: p= 0.005; 5–6 group: p= 0.001) (Figures 2B, C).
Peiminine Suppresses the Resorptive Activity of OCs
To further demonstrate the ability of peiminine to disrupt OC resorption, BMMs were seeded on bone slices and treated with or without varying concentrations of peiminine (5 and 10 μmol/L) together with M-CSF (50 ng/ml) and GST-rRANKL (50 ng/ml). Then, the freeze-dried bone slices were observed by SEM, and the resorption area was measured with ImageJ.
Compared to the control, the non-treatment group, induced by GST-rRANKL, was expected to have the maximum number of OCs and to exhibit the most obvious effect on resorption. Owing to the inhibitory effect of peiminine on OC function, the bone slices in the intervention group were expected to have a smaller resorption area. According to the SEM results and analysis of the data shown in Figures 3A, B, the peiminine-free group had the largest resorption pit area, and the resorption area decreased as the drug concentration increased (5 μmol/L: p= 0.0071; 10 μmol/L: p= 0.0005). The results obtained from bone slices were consistent with our hypothesis.
Figure 3 OC resorption is inhibited by peiminine. (A) Representative images of the bone slice resorption areas in the different groups. BMMs in the first group (control) were neither induced by RANKL nor treated with peiminine; BMMs in the second group were induced by RANKL but not treated with peiminine; and BMMs in the third and fourth groups were induced by RANKL and treated with peiminine at concentrations of 5 µmol/L and 10 µmol/L, respectively. (B) The bone slice resorption areas in all groups were quantitatively analyzed. n= 3, **P < 0.01, ***P < 0.001.
Peiminine Downregulates Formation- and Function-Related Genes
The expression levels of genes critical for RANKL-induced OC differentiation and function, including NFATc1, c-Fos, Acp5 (TRAP), ATP6V0D2, DC-STAMP, and TNF, were analyzed by qRT-PCR to further investigate the mechanism underlying the inhibitory effect of peiminine. Compared with those in the control group, the expression levels of OC-related genes in the RANKL-treated group were substantially elevated. The expression levels of genes related to OC function, such as CTSK (5 μmol/L: p= 0.0082; 10 μmol/L: p= 0.0040) and Acp5 (5 μmol/L: p= 0.0120; 10 μmol/L: p= 0.0005) (Figures 4A, B), and fusion-related genes, such as ATP6v0d2 (5 μmol/L: p= 0.0263; 10 μmol/L: p= 0.0039) and DC-STAMP (5 μmol/L: p= 0.0246; 10 μmol/L: p= 0.0041) (Figures 4C, D), were detected in cells treated with peiminine at concentrations of 5 and 10 μmol/L.
Figure 4 Osteoclastogenesis-related genes are downregulated by peiminine. (A) CTSK, (B) ACP-5, (C) V-ATPase-d2 (ATP6V0D2), (D) DC-STAMP, (E) NFATc1, (F) c-Fos, and (G) TNFRSF11. GAPDH was selected as the control gene. n= 3, *P < 0.05, **P < 0.01, ***P < 0.001.
Similarly, after peiminine intervention, genes related to OC formation (NFATc1 and c-Fos) were downregulated (NFATc1: 5 μmol/L: p= 0.2051; 10 μmol/L: p= 0.451; c-Fos: 5 μmol/L: p= 0.0158; 10 μmol/L: p= 0.0061) (Figures 4E, F). In addition, the expression of the TNFRSF11 gene, which encodes the RANK protein, was inhibited by peiminine (5 μmol/L: p= 0.1065; 10 μmol/L: p= 0.0119) (Figure 4G). These results confirm that peiminine indeed inhibited the RANKL-induced differentiation and function of OCs.
Peiminine Suppresses the Expression of Critical Proteins of RANKL-Induced OCs
The Western blot results were consistent with the qRT-PCR results, demonstrating that peiminine effectively inhibited the expression of essential genes and proteins related to OC differentiation and thereby reduced the expression of downstream genes and proteins associated with OC function. The expression levels of a series of critical factors in the control and experimental groups were measured by Western blot, and the results are shown in Figure 5A.
Figure 5 c-Fos, NFATc1 and downstream proteins are suppressed by peiminine. (A) Western blots analysis of the integrin β3, CTSK, V-ATPase-d2, NFATc1, and c-Fos expression induced by treatment with RANKL (50 ng/mL) for 0, 1, 3, and 5 days in the presence or absence of peiminine (10 μmol/L). Quantitative analysis of the differential expression levels of (B) integrin β3 (n= 5), (C) CTSK (n= 3), (D) V-ATPase-d2 (n= 3), (E) NFATc1 (n= 3), and (F) c-Fos (n= 3). The β-actin was selected as the control protein. *P < 0.05, **P < 0.01.
As mentioned previously, integrin β3, CTSK, and ATP6v0d2 are critical for OC function, and their protein expression levels were reduced in cells treated with peiminine (integrin β3: 0-day: p= 0.9161; 1-day: p= 0.6606; 3-day: p= 0.0373; 5-day: p= 0.0306; CTSK: 0-day: p= 0.8770; 1-day: p= 0.9627; 3-day: p= 0.0167; 5-day: p= 0.0028; ATP6v0d2: 0-day: p= 0.9432; 1-day: p= 0.8401; 3-day: p= 0.0440; 5-day: p= 0.0055) (Figures 5B–D).
NFATc1 and c-Fos, regulatory factors upstream of the abovementioned proteins, were also remarkably downregulated by peiminine in the 3- and 5-day groups (NFATc1: 0-day: p= 0.6205; 1-day: p= 0.9749; 3-day: p= 0.0031; 5-day: p= 0.0117; c-Fos: 0-day: p= 0.1781; 1-day: p= 0.7359; 3-day: p= 0.0296; 5-day: p= 0.0152) (Figures 5E, F).
The NF-κB and ERK1/2 Signaling Pathways Are the Potential Targets of Peiminine
A key molecular event of early RANKL-induced osteoclastogenesis is the activation of NF-κB (28, 29), and activated NF-κB is an integral upstream regulator of NFATc1 (30). As shown in Figure 6B, the levels of NF-κB were notably downregulated by peiminine in the presence of RANKL for 10 min (p= 0.0097), 20 min (p= 0.0043), 30 min (p= 0.0195), and 60 min (p= 0.0324). As shown in Figure 6C, the level of Phosphorylated NF-κB (p-NF-κB) was also decreased by peiminine (p= 0.0083).
Figure 6 Peiminine interferes with the NF-κB and ERK1/2 pathways. (A) Western blot analysis of NF-κB, p-iκB, p-NF-κB, p-ERK1/2, and p-P38 in cells treated with RANKL (50 ng/mL) for different amounts of time (0, 10, 20, 30, and 60 min) in the presence or absence of peiminine (10 μmol/L). Quantitative analysis of the differential expression levels of (B) NF-κB (n= 3), (C) p-NF-κB (n= 4), (D) p-iκB (n= 4), (E) p-ERK1/2 (n= 3), (F) p-P38 (n= 3). β-tublin was selected as the control protein for the normalization of p-iκB, NF-κB, p-NF-κB, and the ERK1/2 for p-ERK1/2, the P38 for p-P38. *P < 0.05, **P < 0.01, ***P < 0.001.
As an important upstream regulator, iκB can prevent the entry of NF-κB into the nucleus; however, during the process of OC differentiation, iκB is phosphorylated by the combination of RANK and RANKL (31). Figure 6D shows that peiminine obviously reduced the expression of p-iκB at 20 min (p= 0.0388), 30 min (p= 1.42687E-05), and 60 min (p= 0.0031) and consequently diminished the levels of p-NF-κB and NF-κB. These findings suggested that peiminine inhibited the NF-κB pathway and thus suppressed OC differentiation and function.
Moreover, MAPK signaling pathways are important regulators of downstream activation (16, 32). We found that the levels of p-ERK1/2 were decreased in cells treated with peiminine for 20 min (p= 0.0166), 30 min (p= 0.0154), and 60 min (p= 0.0208). However, peiminine had no significant effect on the p-P38 level (Figures 6E, F).
Peiminine Plays a Role of Alleviation Against Bone Loss In Vivo
Animal experiments were performed to evaluate the bio-effect of peiminine in vivo. μCT and histomorphometric analyses showed that peiminine obviously alleviated the resorption of bone caused by OCs (Figure 7A). The BV/TV was obviously higher in the peiminine-treated group than in the OVX group (p= 1.03253E-05) (Figure 7B). Similarly, the Tb. N and Tb. Th were higher in the peiminine-treated group than in the OVX group (Tb.N: p= 6.72736E-05; Tb.Th: p= 2.21584E-05) (Figures 7C, D), while the Tb. Sp in the intervention group was lower than that in OVX group (p= 1.55671E-07) (Figure 7E).
Figure 7 Peiminine ameliorates the systematic bone loss induced by OVX. (A) Computer-generated 3D high-resolution micro-CT image of the femur microstructure. Quantitative measurements of (B) BV/TV, (C) Tb. N, (D) Tb. Th, and (E) Tb. Sp in the control group (sham), non-treatment group (OVX), and treatment group (OVX+peiminine). n= 10, ***P < 0.001.
The histomorphometric analysis results further supported the findings presented above. H&E staining indicated the distribution of OCs and trabecular bone in vivo, and the result was consistent with that obtained by μCT analysis. Then, OCs at corresponding positions were stained, revealing that sections from peiminine-treated OVX mice had significantly fewer TRAP-positive cells than those from untreated OVX mice (Figure 8A). The OC. S/BS (p= 0.004493691) and OC. N/BS (p= 0.000363396) results also indicated that peiminine inhibited osteoclastogenesis in bone tissue (Figures 8B, C).
Figure 8 Peiminine had no bio-toxicity and ameliorated the bone loss induced by OVX by inhibiting osteoclastogenesis in vivo. (A) Representative H&E and TRAP staining images of decalcified bones from mice in the sham, OVX, and peiminine (10 mg/kg) treatment groups. (B) Representative H&E staining images of kidneys and livers of mice from the control and experimental groups. Quantitative measurements of (B) OC. S/BS; (C) OC. N/BS, in the control group (Sham), non-treatment group (OVX), and treatment group (OVX + peiminine). n= 5, **P < 0.01, ***P < 0.001. (D) Representative H&E staining images of kidneys and livers of mouse from control and experimental groups.
Additionally, H&E staining of liver and kidney tissues harvested from the mice showed no lesions in any of the groups (Figure 8D). The lack of peiminine toxicity in vivo corresponded with the results of the CCK-8 assay described in the section Peiminine Is Not Toxic in BMMs and Suppresses OC Formation and Fusion Induced by RANKL.
Discussion
In this study, TRAP staining was used as the major determination method to demonstrate many indices of osteoclastogenesis, because TRAP is associated with oxidative stress and a crucial indicator of OCs (33). According to our results, under the premise of peiminine’s biosafety, we verified peiminine’s inhibitory effect in different concentrations and stages. Furthermore, the fluorescence staining and bone slice resorption results strengthen the TRAP staining results and together show that peiminine suppressed both OC fusion and function.
The following experiments were carried out to confirm the conclusions above at the molecular level. The role of NFATc1 is critical throughout osteoclastogenesis (34), and according to previous research, c-Fos is the indispensable bridge between RANK and NFATc1 (17, 35, 36). As shown in Figures 4 and 5, the levels of the gene TNFRSF11, which encodes for RANK, and the genes NFATc1 and c-Fos were in decline within the groups treated with peiminine. Results above suggest that peiminine might affect the whole RANK-NFATc1 pathway. Therefore, it can be speculated that peiminine decreases the levels of downstream factors, including CTSK, and Integrinβ3, which are crucial for OCs’ resorption (37–39); as well as DC-STAMP and ATP6v0d2, which are indispensable in OCs’ cellular fusion and maturation (3, 40–43).
The activation of NF-κB is an important event that occurs in the early stage of RANKL-induced OC differentiation and is vital for the activation of NFATc1 (44). NF-κB is mainly present in the cytosol in the form of a dimer consisting of iκB and NF-κB, and iκB can prevent NF-κB from entering the nuclei (17, 45). RANKL can induce the phosphorylation of iκB and lead to the degradation of iκB. NF-κB is activated in the absence of iκB, and p-NF-κB enters the nucleus and is involved in the activation of NFATc1 (32). As shown in Figures 6A, C, D, peiminine downregulated the expression of NF-κB and p-NF-κB, suggesting that it has an inhibitory effect on NFATc1. We also found that peiminine significantly decreased the level of p-iκB, suggesting that it suppresses the degradation of iκB by inhibiting iκB phosphorylation. This phenomenon explains why the levels of NF-κB and p-NF-κB were reduced in the presence of peiminine.
MAPK pathways, including ERK, JNK, and P38, are associated with OC formation and function (36, 46), and ERK is indispensable for OC survival (18, 35). We therefore assessed these two signaling pathways, revealing that peiminine downregulated ERK1/2 in the early stage of osteoclastogenesis but did not affect the expression of p-P38. Peiminine inhibited osteoclastogenesis and obviously prevented bone loss in OVX mice, most likely by interfering with the NF-κB, ERK and c-Fos-NFATc1 pathways (Figure 9).
Figure 9 Schematic diagram of how peiminine suppresses RANKL-induced osteoclastogenesis.
Estrogen has the ability to block osteoclastogenesis and increase OC apoptosis, and the withdrawal of estrogen increases the number of OCs and promotes bone resorption (47). Thus, we used OVX mouse as the experimental animal model. Animal experiments further supported the results in vitro. Because peiminine can presumably alleviate estrogen deficiency-induced osteoclastogenesis in vivo. The μCT and histological analysis results suggested that peiminine effectively decreased the level of osteoporosis in OVX mice, as relatively mild bone loss was observed in these mice treated with peiminine. Besides, the biosafety of peiminine was reconfirmed by animal experiments, as none of the mice injected with peiminine exhibited an abnormal reaction or hypersensitivity, demonstrating its safety.
In this study, we assessed the alleviating effect of peiminine in vivo after systemic administration, but there is room for improvement. For example, whether the circumstances of systemic peiminine administration affect bone homeostasis or cause side effects remains unknown. The inclusion of an extra sham-operated group of mice treated with peiminine could help to assess the effect of the drug in the steady state. Additionally, the serum detection of bone turnover markers, such as CTX, OPG, P1NP, and RANKL, after peiminine treatment would presumably further elucidate its mechanism of action.
In addition, the mode of peiminine needs to be further investigated. In this study, OVX mice were treated before the induction of osteoporosis, which indicated the alleviating effect of peiminine on bone loss, but whether peiminine can ameliorate previous bone loss remains to be determined. In the future, we plan to administer peiminine to osteoporotic mice to study its therapeutic effect upon osteoporosis. It is also important to explore the effects of the drug on mice undergoing long-term treatment, as these experiments can provide more information on the long-term impacts of peiminine on bone quality and potential side effects and thereby aid the development of more scientific therapeutic strategies.
In the future, we hope to study additional dosing strategies. A newly developed smart nanosacrificial layer was shown to precisely target and inhibit osteoclast function. Nanomaterials modified by tetracycline with bone-targeting properties can be used to encapsulate intervening drugs, thereby yielding better targeted drug delivery than that achieved via systemic administration (48). This represents a promising research direction for the application of peiminine in the future.
Conclusion
This study demonstrates that peiminine, a natural herb-extracted compound, can inhibit the formation and function of OCs via multiple targets and is therefore a promising novel therapeutic agent for osteoporosis.
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding authors.
Ethics Statement
The animal study was reviewed and approved by Laboratory Animal Center of Sir Run Run Shaw Affiliated Hospital of Zhejiang University School of Medicine.
Author Contributions
MZ and SW contributed to conception. MZ, LS, and TW designed the study, and MZ wrote the first draft of the manuscript. WX, JZ, and YW organized the database. YG, RY, and YC performed the statistical analysis. BZ, ZW, and JZ wrote sections of the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This project was supported by the National Natural Science Foundation of China (Grant Nos. 81572207, 81201435, 82101647), Natural Science Fund of Zhejiang Province (LQ20H060005) Medical Health Science and Technology Project of Zhejiang Provincial Health Commission (2021436226), Health Commission of Shanxi Province (Grant No. 2020075), and the Public Projects of Zhejiang Province (LGF19H060013).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1. Armas LA, Recker RR. Pathophysiology of Osteoporosis: New Mechanistic Insights. Endocrinol Metab Clin North Am (2012) 41(3):475–86. doi: 10.1016/j.ecl.2012.04.006
2. Coughlan T, Dockery F. Osteoporosis and Fracture Risk in Older People. Clin Med (Lond) (2014) 14(2):187–91. doi: 10.7861/clinmedicine.14-2-187
3. Chen X, Wang Z, Duan N, Zhu G, Schwarz EM, Xie C. Osteoblast-Osteoclast Interactions. Connect Tissue Res (2018) 59(2):99–107. doi: 10.1080/03008207.2017.1290085
4. Judd HL, Meldrum DR, Deftos LJ, Henderson BE. Estrogen Replacement Therapy: Indications and Complications. Ann Intern Med (1983) 98(2):195–205. doi: 10.7326/0003-4819-98-2-195
5. Ticconi C, Pietropolli A, Piccione E. Estrogen Replacement Therapy and Asthma. Pulm Pharmacol Ther (2013) 26(6):617–23. doi: 10.1016/j.pupt.2013.08.004
6. Maraka S, Kennel KA. Bisphosphonates for the Prevention and Treatment of Osteoporosis. BMJ (2015) 351:h3783. doi: 10.1136/bmj.h3783
7. Jin H, Wang Q, Chen K, Xu K, Pan H, Chu F, et al. Astilbin Prevents Bone Loss in Ovariectomized Mice Through the Inhibition of RANKL-Induced Osteoclastogenesis. J Cell Mol Med (2019) 23(12):8355–68. doi: 10.1111/jcmm.14713
8. Jin H, Yao L, Chen K, Liu Y, Wang Q, Wang Z, et al. Evodiamine Inhibits RANKL-Induced Osteoclastogenesis and Prevents Ovariectomy-Induced Bone Loss in Mice. J Cell Mol Med (2019) 23(1):522–34. doi: 10.1111/jcmm.13955
9. Wang Q, Yao L, Xu K, Jin H, Chen K, Wang Z, et al. Madecassoside Inhibits Estrogen Deficiency-Induced Osteoporosis by Suppressing RANKL-Induced Osteoclastogenesis. J Cell Mol Med (2019) 23(1):380–94. doi: 10.1111/jcmm.13942
10. Ruan X, Yang L, Cui WX, Zhang MX, Li ZH, Liu B, et al. Optimization of Supercritical Fluid Extraction of Total Alkaloids, Peimisine, Peimine and Peiminine From the Bulb of Fritillaria Thunbergii Miq, and Evaluation of Antioxidant Activities of the Extracts. Materials (Basel) (2016) 9(7):524–41. doi: 10.3390/ma9070524
11. Gong Q, Li Y, Ma H, Guo W, Kan X, Xu D, et al. Peiminine Protects Against Lipopolysaccharide-Induced Mastitis by Inhibiting the AKT/NF-Kappab, ERK1/2 and P38 Signaling Pathways. Int J Mol Sci (2018) 19(9):2637–49. doi: 10.3390/ijms19092637
12. Chen G, Liu J, Jiang L, Ran X, He D, Li Y, et al. Peiminine Protects Dopaminergic Neurons From Inflammation-Induced Cell Death by Inhibiting the ERK1/2 and NF-kappaB Signalling Pathways. Int J Mol Sci (2018) 19(3):821–33. doi: 10.3390/ijms19030821
13. Miyamoto T. Regulators of Osteoclast Differentiation and Cell-Cell Fusion. Keio J Med (2011) 60(4):101–5. doi: 10.2302/kjm.60.101
14. Amin N, Boccardi V, Taghizadeh M, Jafarnejad S. Probiotics and Bone Disorders: The Role of RANKL/RANK/OPG Pathway. Aging Clin Exp Res (2020) 32(3):363–71. doi: 10.1007/s40520-019-01223-5
15. Tobeiha M, Moghadasian MH, Amin N, Jafarnejad S. RANKL/RANK/OPG Pathway: A Mechanism Involved in Exercise-Induced Bone Remodeling. BioMed Res Int (2020) 2020:6910312. doi: 10.1155/2020/6910312
16. Boyle WJ, Simonet WS, Lacey DL. Osteoclast Differentiation and Activation. Nature (2003) 423(6937):337–42. doi: 10.1038/nature01658
17. Hayden MS, Ghosh S. Signaling to NF-Kappab. Genes Dev (2004) 18(18):2195–224. doi: 10.1101/gad.1228704
18. Koga Y, Tsurumaki H, Aoki-Saito H, Sato M, Yatomi M, Takehara K, et al. Roles of Cyclic AMP Response Element Binding Activation in the ERK1/2 and P38 MAPK Signalling Pathway in Central Nervous System, Cardiovascular System, Osteoclast Differentiation and Mucin and Cytokine Production. Int J Mol Sci (2019) 20(6):1346–68. doi: 10.3390/ijms20061346
19. Chao X, Wang G, Tang Y, Dong C, Li H, Wang B, et al. The Effects and Mechanism of Peiminine-Induced Apoptosis in Human Hepatocellular Carcinoma HepG2 Cells. PloS One (2019) 14(1):e0201864. doi: 10.1371/journal.pone.0201864
20. Lyu Q, Tou F, Su H, Wu X, Chen X, Zheng Z. The Natural Product Peiminine Represses Colorectal Carcinoma Tumor Growth by Inducing Autophagic Cell Death. Biochem Biophys Res Commun (2015) 462(1):38–45. doi: 10.1016/j.bbrc.2015.04.102
21. Du B, Cao L, Wang K, Miu J, Yao L, Xu Z, et al. Peiminine Attenuates Acute Lung Injury Induced by LPS Through Inhibiting Lipid Rafts Formation. Inflammation (2020) 43(3):1110–9. doi: 10.1007/s10753-020-01198-w
22. Guo H, Ji F, Liu B, Chen X, He J, Gong J. Peiminine Ameliorates Bleomycin-Induced Acute Lung Injury in Rats. Mol Med Rep (2013) 7(4):1103–10. doi: 10.3892/mmr.2013.1312
23. Ma X, Liu A, Liu W, Wang Z, Chang N, Li S, et al. Analyze and Identify Peiminine Target EGFR Improve Lung Function and Alleviate Pulmonary Fibrosis to Prevent Exacerbation of Chronic Obstructive Pulmonary Disease by Phosphoproteomics Analysis. Front Pharmacol (2019) 10:737. doi: 10.3389/fphar.2019.00737
24. Zhao B, Shen C, Zheng Z, Wang X, Zhao W, Chen X, et al. Peiminine Inhibits Glioblastoma In Vitro and In Vivo Through Cell Cycle Arrest and Autophagic Flux Blocking. Cell Physiol Biochem (2018) 51(4):1566–83. doi: 10.1159/000495646
25. Luo Z, Zheng B, Jiang B, Xue X, Xue E, Zhou Y. Peiminine Inhibits the IL-1beta Induced Inflammatory Response in Mouse Articular Chondrocytes and Ameliorates Murine Osteoarthritis. Food Funct (2019) 10(4):2198–208. doi: 10.1039/c9fo00307j
26. Chen X, Wang C, Qiu H, Yuan Y, Chen K, Cao Z, et al. Asperpyrone A Attenuates RANKL-Induced Osteoclast Formation Through Inhibiting NFATc1, Ca(2+) Signalling and Oxidative Stress. J Cell Mol Med (2019) 23(12):8269–79. doi: 10.1111/jcmm.14700
27. Zhou L, Liu Q, Yang M, Wang T, Yao J, Cheng J, et al. Dihydroartemisinin, an Anti-Malaria Drug, Suppresses Estrogen Deficiency-Induced Osteoporosis, Osteoclast Formation, and RANKL-Induced Signaling Pathways. J Bone Miner Res (2016) 31(5):964–74. doi: 10.1002/jbmr.2771
28. Anderson DM, Maraskovsky E, Billingsley WL, Dougall WC, Tometsko ME, Roux ER, et al. A Homologue of the TNF Receptor and Its Ligand Enhance T-Cell Growth and Dendritic-Cell Function. Nature (1997) 390(6656):175–9. doi: 10.1038/36593
29. Bourette RP, Rohrschneider LR. Early Events in M-CSF Receptor Signaling. Growth Factors (2000) 17(3):155–66. doi: 10.3109/08977190009001065
30. Asagiri M, Sato K, Usami T, Ochi S, Nishina H, Yoshida H, et al. Autoamplification of NFATc1 Expression Determines Its Essential Role in Bone Homeostasis. J Exp Med (2005) 202(9):1261–9. doi: 10.1084/jem.20051150
31. Jimi E, Takakura N, Hiura F, Nakamura I, Hirata-Tsuchiya S. The Role of NF-kappaB in Physiological Bone Development and Inflammatory Bone Diseases: Is NF-kappaB Inhibition "Killing Two Birds With One Stone"? Cells (2019) 8(12):1636–51. doi: 10.3390/cells8121636
32. Asagiri M, Takayanagi H. The Molecular Understanding of Osteoclast Differentiation. Bone (2007) 40(2):251–64. doi: 10.1016/j.bone.2006.09.023
33. Hayman AR. Tartrate-Resistant Acid Phosphatase (TRAP) and the Osteoclast/Immune Cell Dichotomy. Autoimmunity (2008) 41(3):218–23. doi: 10.1080/08916930701694667
34. Lacey DL, Timms E, Tan HL, Kelley MJ, Dunstan CR, Burgess T, et al. Osteoprotegerin Ligand Is a Cytokine That Regulates Osteoclast Differentiation and Activation. Cell (1998) 93(2):165–76. doi: 10.1016/s0092-8674(00)81569-x
35. Miyazaki T, Katagiri H, Kanegae Y, Takayanagi H, Sawada Y, Yamamoto A, et al. Reciprocal Role of ERK and NF-kappaB Pathways in Survival and Activation of Osteoclasts. J Cell Biol (2000) 148(2):333–42. doi: 10.1083/jcb.148.2.333
36. Matsumoto M, Kogawa M, Wada S, Takayanagi H, Tsujimoto M, Katayama S, et al. Essential Role of P38 Mitogen-Activated Protein Kinase in Cathepsin K Gene Expression During Osteoclastogenesis Through Association of NFATc1 and PU.1. J Biol Chem (2004) 279(44):45969–79. doi: 10.1074/jbc.M408795200
37. Drake MT, Clarke BL, Oursler MJ, Khosla S. Cathepsin K Inhibitors for Osteoporosis: Biology, Potential Clinical Utility, and Lessons Learned. Endocr Rev (2017) 38(4):325–50. doi: 10.1210/er.2015-1114
38. Geoghegan IP, Hoey DA, McNamara LM. Integrins in Osteocyte Biology and Mechanotransduction. Curr Osteoporos Rep (2019) 17(4):195–206. doi: 10.1007/s11914-019-00520-2
39. Hynes RO. Integrins: Versatility, Modulation, and Signaling in Cell Adhesion. Cell (1992) 69(1):11–25. doi: 10.1016/0092-8674(92)90115-s
40. Chiu YH, Ritchlin CT. DC-STAMP: A Key Regulator in Osteoclast Differentiation. J Cell Physiol (2016) 231(11):2402–7. doi: 10.1002/jcp.25389
41. Islam R, Bae HS, Yoon WJ, Woo KM, Baek JH, Kim HH, et al. Pin1 Regulates Osteoclast Fusion Through Suppression of the Master Regulator of Cell Fusion DC-STAMP. J Cell Physiol (2014) 229(12):2166–74. doi: 10.1002/jcp.24679
42. Lee SH, Rho J, Jeong D, Sul JY, Kim T, Kim N, et al. V-ATPase V0 Subunit D2-Deficient Mice Exhibit Impaired Osteoclast Fusion and Increased Bone Formation. Nat Med (2006) 12(12):1403–9. doi: 10.1038/nm1514
43. Mensah KA, Ritchlin CT, Schwarz EM. RANKL Induces Heterogeneous DC-STAMP(lo) and DC-STAMP(hi) Osteoclast Precursors of Which the DC-STAMP(lo) Precursors Are the Master Fusogens. J Cell Physiol (2010) 223(1):76–83. doi: 10.1002/jcp.22012
44. Takatsuna H, Asagiri M, Kubota T, Oka K, Osada T, Sugiyama C, et al. Inhibition of RANKL-Induced Osteoclastogenesis by (-)-DHMEQ, a Novel NF-kappaB Inhibitor, Through Downregulation of Nfatc1. J Bone Miner Res (2005) 20(4):653–62. doi: 10.1359/JBMR.041213
45. Ghosh S, Karin M. Missing Pieces in the NF-kappaB Puzzle. Cell (2002) 109(Suppl):S81–96. doi: 10.1016/s0092-8674(02)00703-1
46. Matsumoto M, Sudo T, Saito T, Osada H, Tsujimoto M. Involvement of P38 Mitogen-Activated Protein Kinase Signaling Pathway in Osteoclastogenesis Mediated by Receptor Activator of NF-Kappa B Ligand (RANKL). J Biol Chem (2000) 275(40):31155–61. doi: 10.1074/jbc.M001229200
47. Pacifici R. Estrogen, Cytokines, and Pathogenesis of Postmenopausal Osteoporosis. J Bone Miner Res (1996) 11(8):1043–51. doi: 10.1002/jbmr.5650110802
Keywords: peiminine, osteoclast, NFATc1, NF-κB, osteoporosis
Citation: Zhu M, Xu W, Jiang J, Wang Y, Guo Y, Yang R, Chang Y, Zhao B, Wang Z, Zhang J, Wang T, Shangguan L and Wang S (2021) Peiminine Suppresses RANKL-Induced Osteoclastogenesis by Inhibiting the NFATc1, ERK, and NF-κB Signaling Pathways. Front. Endocrinol. 12:736863. doi: 10.3389/fendo.2021.736863
Received: 06 July 2021; Accepted: 02 September 2021;
Published: 24 September 2021.
Edited by:
Chandi C. Mandal, Central University of Rajasthan, IndiaReviewed by:
Florence Figeac, Odense University Hospital, DenmarkCiro Menale, University of Naples Federico II, Italy
Copyright © 2021 Zhu, Xu, Jiang, Wang, Guo, Yang, Chang, Zhao, Wang, Zhang, Wang, Shangguan and Wang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Shaowei Wang, ZHJlYW1rb2JlQDE2My5jb20=; Liqin Shangguan, bHFzaGFuZ2d1YW5Aemp1LmVkdS5jbg==; Te Wang, Mjg5NzI2MjY5QHFxLmNvbQ==
†These authors have contributed equally to this work